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Clinical experience with a simple algorithm for plerixafor utilization in autologous stem cell mobilization.

Authors :
Chen, A I
Bains, T
Murray, S
Knight, R
Shoop, K
Bubalo, J
Fowler, C
Slater, S
Maziarz, R T
Source :
Bone Marrow Transplantation; Dec2012, Vol. 47 Issue 12, p1526-1529, 4p, 3 Charts, 2 Graphs
Publication Year :
2012

Abstract

Plerixafor augments PBSC collection, but the optimal approach for incorporating it into mobilization is uncertain. Forty-nine consecutive patients mobilized with G-CSF alone were analyzed, and a day 4 peripheral blood CD34<superscript>+</superscript> cell count of 0.015/ml was found to predict for a day 5 apheresis yield of 2 × 10<superscript>6</superscript> CD34<superscript>+</superscript> progenitors/kg, our institutional minimum necessary for a single autologous transplant. On the basis of this relationship, a clinical guideline was developed which recommended pre-emptive use of plerixafor if the day 4 peripheral blood CD34<superscript>+</superscript> cell count was between 0.005 and 0.015/ml. A total of 166 consecutive subjects with lymphoma or plasma cell dyscrasias underwent G-CSF mobilization after adoption of this care pathway, and the mobilization failure rate was only 7% in patients managed per guideline. The median PBSC yield was 6.3 × 10<superscript>6</superscript> CD34<superscript>+</superscript> progenitors/kg with G-CSF (day 4 peripheral blood CD34<superscript>+</superscript> cell>0.015/ml) and 4.9 × 10<superscript>6</superscript> CD34<superscript>+</superscript> progenitors/kg with G-CSF+plerixafor (day 4 peripheral blood CD34<superscript>+</superscript> cell 0.005-0.015/ml). The median number of days of apheresis was 2 in both groups. This clinical guideline is an effective mobilization algorithm that minimizes mobilization failures, reduces poor apheresis yields, does not require risk factor identification and is simple to implement. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
02683369
Volume :
47
Issue :
12
Database :
Complementary Index
Journal :
Bone Marrow Transplantation
Publication Type :
Academic Journal
Accession number :
83846419
Full Text :
https://doi.org/10.1038/bmt.2012.74